Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
310
Gene name Gene Name - the full gene name approved by the HGNC.
Annexin A7
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ANXA7
Synonyms (NCBI Gene) Gene synonyms aliases
ANX7, SNX, SYNEXIN
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q22.2
Summary Summary of gene provided in NCBI Entrez Gene.
Annexin VII is a member of the annexin family of calcium-dependent phospholipid binding proteins.The Annexin VII gene contains 14 exons and spans approximately 34 kb of DNA. An alternatively spliced cassette exon results in two mRNA transcripts of 2.0 and
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT023283 hsa-miR-122-5p Proteomics 21750653
MIRT048217 hsa-miR-196a-5p CLASH 23622248
MIRT043161 hsa-miR-324-5p CLASH 23622248
MIRT439134 hsa-miR-10b-5p 3'LIFE 25074381
MIRT439134 hsa-miR-10b-5p 3'LIFE 25074381
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001786 Function Phosphatidylserine binding IBA
GO:0003723 Function RNA binding HDA 22681889
GO:0005178 Function Integrin binding IPI 24007983
GO:0005509 Function Calcium ion binding IEA
GO:0005515 Function Protein binding IPI 9268363, 12445460, 17699613
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
186360 545 ENSG00000138279
Protein
UniProt ID P20073
Protein name Annexin A7 (Annexin VII) (Annexin-7) (Synexin)
Protein function Calcium/phospholipid-binding protein which promotes membrane fusion and is involved in exocytosis.
PDB 8W5S
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00191 Annexin 189 254 Annexin Family
PF00191 Annexin 261 326 Annexin Family
PF00191 Annexin 344 410 Annexin Family
PF00191 Annexin 420 485 Annexin Family
Tissue specificity TISSUE SPECIFICITY: Isoform 1 is expressed in brain, heart and skeletal muscle. Isoform 2 is more abundant in liver, lung, kidney, spleen, fibroblasts and placenta. {ECO:0000269|PubMed:1825209}.
Sequence
MSYPGYPPTGYPPFPGYPPAGQESSFPPSGQYPYPSGFPPMGGGAYPQVPSSGYPGAGGY
PAPGGYPAPGGYPGAPQPGGAPSYPGVPPGQGFGVPPGGAGFSGYPQPPSQSYGGGPAQV
PLPGGFPGGQMPSQYPGGQPTYPSQINTDSFSSYPVFSPVSLDYSSEPATVTQVTQGTIR
PAANFDAIRDAEILRKAMKGFGTDEQAIVDVVANRSNDQRQKIKAAFKTSYGKDLIKDLK
SELSGNMEELILAL
FMPPTYYDAWSLRKAMQGAGTQERVLIEILCTRTNQEIREIVRCYQ
SEFGRDLEKDIRSDTSGHFERLLVSM
CQGNRDENQSINHQMAQEDAQRLYQAGEGRLGTD
ESCFNMILATRSFPQLRATMEAYSRMANRDLLSSVSREFSGYVESGLKTI
LQCALNRPAF
FAERLYYAMKGAGTDDSTLVRIVVTRSEIDLVQIKQMFAQMYQKTLGTMIAGDTSGDYRR
LLLAI
VGQ
Sequence length 488
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Amyotrophic lateral sclerosis  
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